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Decoding the Future of Multiple Myeloma: A Sneak Peek into the Top Abstracts of Multiple Myeloma at 2024 European Hematology Association (EHA) Congress

Multiple Myeloma Top Abstracts | EHA 2024

The market for multiple myeloma is rapidly evolving, and current and emerging key players face the biggest risk due to this high degree of innovation. Antibody-drug-conjugates (ADCs), CAR-T cell treatments, and bispecific antibodies are just a few of the novel modes of action that have recently entered the market for the treatment of Multiple Myeloma.

In frontline multiple myeloma clinical studies, DARZALEX was successful and is now considered the standard of therapy. DARZALEX has outperformed rivals' expectations in terms of effectiveness and safety and is expected to rule the multiple myeloma market.

A second CD38 antibody called SARCLISA has been approved for treating multiple myeloma. SARCLISA continues its rapid acceptance in key markets. But DARZALEX has an advantage over SARCLISA of more than four years. Both monoclonal antibodies are competing against one another in a quadruplet regimen in both transplant-eligible and ineligible settings. The two CD38 antibodies are also close to a showdown in patients who are not eligible for transplant. This wave of evidences for the CD38-RVd combinations comes from studies in the transplant-eligible group.

Multiple myeloma is a promising therapeutic target due to the widespread expression of BCMA on myeloma cells. The field of BCMA-targeting drugs in multiple myeloma has undergone significant advancement. Introduction of CAR-T cell therapies ABECMA and CARVYKTI, and most recently TECVAYLI, are examples of the rise of the BCMA space in multiple myeloma. 

Top pharmaceutical companies like Bristol Myers Squibb, Sanofi, AbbVie, GlaxoSmithKline, Gracell Biotechnologies (Astrazeneca), Johnson & Johnson Innovative Medicine, Regeneron, CARsgen, Roche and others are gearing up for the conference, ready to present initial, updated and final results. The upcoming session is highly anticipated for its unveiling of primary results from the Phase III IMROZ study, hoping to offer a potential treatment option for transplant-ineligible newly diagnosed multiple myeloma patients in combination with VRD. Additionally, the results of Ciltacabtagene Autoleucel from CARTITUDE-2 trial and, Belantamab results from DREAMM-7 will be of much interest during the EHA 2024.

In this context, DelveInsight has meticulously compiled a list of the top oral presentation abstracts related to multiple myeloma. These abstracts are on the verge of potentially transforming patient care in the future. They carry the potential for substantial progress, aiming to positively impact the treatment landscape of multiple myeloma.

Multiple Myeloma Key Abstracts

Therapy

Name

Company

Class

Abstract ID

Presentation Type

Session Date/

Time

Abstract Title

Author

Idecabtagene Vicleucel

BCMA-CAR-T

S208

Oral Presentation

June 15/

(17:15 - 17:30 CEST)

IDECABTAGENE VICLEUCEL (IDE-CEL) IN PATIENTS (PTS) WITH CLINICAL HIGH-RISK EARLY RELAPSE MULTIPLE MYELOMA (MM) WITHOUT FRONT-LINE (1L) AUTOLOGOUS STEM CELL TRANSPLANTATION (ASCT): KARMMA-2 COHORT 2B

Xavier Leleu

ABBV-383

CD3 x BCMA bispecific antibody

S211

Oral Presentation

June 15/

(8:30 – 9:30 CEST)

EFFICACY, SAFETY, AND DETERMINATION OF RP2D OF ABBV-383, A BCMA BISPECIFIC ANTIBODY, IN PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA (RRMM).

Katja Weisel*

Isatuximab

Anti-CD38 mAb

S100

Oral Presentation

June 15, 2024 (14:45 - 16:15 CEST)

PHASE 3 STUDY RESULTS OF ISATUXIMAB, BORTEZOMIB, LENALIDOMIDE, AND DEXAMETHASONE (ISA-VRD) VERSUS VRD FOR TRANSPLANT-INELIGIBLE PATIENTS WITH NEWLY DIAGNOSED MULTIPLE MYELOMA (IMROZ)

Thierry Facon

GC012F

CD19 x BCMA bispecific antibody

S200

Oral Presentation

June 15, 2024 (11:30 - 11:45 CEST)

A PHASE I OPEN-LABEL SINGLE-ARM STUDY OF DUAL TARGETING BCMA AND CD19 FASTCAR-T (GC012F) AS FIRST-LINE THERAPY FOR TRANSPLANT-ELIGIBLE NEWLY DIAGNOSED HIGH-RISK MULTIPLE MYELOMA

Juan Du

Linvoseltamab

CD3 x BCMA bispecific antibody

S212

Oral Presentation

June 16, 2024 (12:00 - 12:15 CEST)

LINVOSELTAMAB IN PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA IN THE LINKER-MM1

STUDY: DEPTH AND DURABILITY OF RESPONSE AT 14-MONTH MEDIAN FOLLOW-UP

Suzanne Lentzsch

Ciltacabtagene Autoleucel ± Lenalidomide

BCMA-CAR-T

S205

Oral Presentation

June 15, 2024 (16:30 - 16:45 CEST)

CILTACABTAGENE AUTOLEUCEL ± LENALIDOMIDE MAINTENANCE IN NEWLY DIAGNOSED MULTIPLE MYELOMA WITH SUBOPTIMAL RESPONSE TO FRONTLINE AUTOLOGOUS STEM CELL TRANSPLANT: CARTITUDE-2 COHORT D

Wilfried Roeloffzen

Equecabtagene Autoleucel

BCMA-CAR-T

S206

Oral Presentation

June 15, 2024 (16:45 - 17:00 CEST)

EQUE-CEL, A NOVEL FULLY HUMAN BCMA-TARGETING CAR-T THERAPY IN PATIENTS WITH HIGH RISK NEWLY DIAGNOSED MULTIPLE MYELOMA

Lijuan Chen

Zevorcabtagene Autoleucel

BCMA-CAR-T

S209

Oral Presentation

June 15;2024

(17:30 - 17:45 CEST)

PHASE 2 STUDY OF FULLY HUMAN BCMA-TARGETING CAR-T CELLS (ZEVORCABTAGENE AUTOLEUCEL) IN

PATIENTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA

Wenming Chen

Isatuximab

Anti-CD38 mAb

S203

Oral Presentation

June 15, 2024 (12:15 - 12:30 CEST)

RANDOMIZED PHASE 3 STUDY OF ISATUXIMAB (ISA) PLUS LENALIDOMIDE AND DEXAMETHASONE (RD) WITH

BORTEZOMIB (V) VERSUS ISARD IN PATIENTS WITH NEWLY DIAGNOSED TRANSPLANT INELIGIBLE MULTIPLE

MYELOMA (NDMM TI)

Xavier Leleu

Isatuximab

Anti-CD38 mAb

S202

Oral Presentation

June 15, 2024 (12:00 - 12:15 CEST)

ISATUXIMAB, LENALIDOMIDE, BORTEZOMIB AND DEXAMETHASONE FOR NEWLY-DIAGNOSED, TRANSPLANTELIGIBLE MULTIPLE MYELOMA: POST TRANSPLANTATION INTERIM ANALYSIS OF THE RANDOMIZED PHASE III

GMMG-HD7 TRIAL

Marc S. Raab

Daratumumab

Anti-CD38 mAb

S201

Oral Presentation

June 15, 2024 (11:45 - 12:00 CEST)

DARATUMUMAB + BORTEZOMIB/LENALIDOMIDE/DEXAMETHASONE IN TRANSPLANT-ELIGIBLE PATIENTS WITH

NEWLY DIAGNOSED MULTIPLE MYELOMA: ANALYSIS OF MINIMAL RESIDUAL DISEASE IN THE PERSEUS TRIAL

Pieter Sonneveld

Belantamab

BCMA- ADC

S214

Oral Presentation

June 16, 2024 (12:30 - 12:45 CEST)

RESULTS FROM DREAMM-7 A RANDOMIZED PHASE 3 STUDY OF BELANTAMAB MAFODOTIN + BORTEZOMIB,

AND DEXAMETHASONE VS DARATUMUMAB + BORTEZOMIB, AND DEXAMETHASONE IN RELAPSED/REFRACTORY

MULTIPLE MYELOMA

Maria-Victoria Mateos

Belantamab

BCMA- ADC

LB3440

Oral Presentation

June 16, 2024 (10:00 - 10:15 CEST)

RESULTS FROM THE RANDOMIZED PHASE 3 DREAMM-8 STUDY OF BELANTAMAB MAFODOTIN PLUS POMALIDOMIDE AND DEXAMETHASONE VS POMALIDOMIDE PLUS BORTEZOMIB AND DEXAMETHASONE IN REPALPSED/REFRACTORY MULTIPLE MYELOMA

Meletios Dimopoulos

Cevostamab

CD3 x FCRH5 bispecific antibody

S210

Oral Presentation

16 June, 2024 (11:30 - 11:45 CEST)

CEVOSTAMAB IN PATIENTS WITH RRMM WHO ARE TRIPLE-CLASS REFRACTORY AND HAVE RECEIVED A PRIOR BCMA-TARGETED ADC OR CAR T-CELL: INITIAL RESULTS FROM THE PHASE I/II CAMMA 2 STUDY

Shaji Kumar

 

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Executive Summary

The market for multiple myeloma is rapidly evolving, and current and emerging key players face the biggest risk due to this high degree of innovation.

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